Inhibicijski faktor migracije makrofaga

Inhibitorni faktor migracije makrofaga (MIF), znan i kao inhibitorni faktor glikozilacije (GIF), L-dopahrom-izomeraza ili fenilpiruvat-tautomeraza jest protein/enzim koji je kod ljudi kodiran genom MIF sa hromosoma 22.[5][6] MIF je važan regulator urođene imunosti.[7] Natporodica proteina MIF također uključuje drugog člana s funkcionalno srodnim svojstvima, D-dopahrom-tautomerazu (D-DT).[8]Površinski receptor za MIF je CD74.[9]

Inhibicijski faktor migracije makrofaga
Dostupne strukture
PDBPretraga ortologa: PDBe RCSB
Spisak PDB ID kodova

1CA7, 1CGQ, 1GCZ, 1GD0, 1GIF, 1LJT, 1MIF, 1P1G, 2OOH, 2OOW, 2OOZ, 3B9S, 3CE4, 3DJH, 3DJI, 3HOF, 3IJG, 3IJJ, 3JSF, 3JSG, 3JTU, 3L5P, 3L5R, 3L5S, 3L5T, 3L5U, 3L5V, 3SMB, 3SMC, 3U18, 4ETG, 4EUI, 4EVG, 4F2K, 4GRN, 4GRO, 4GRP, 4GRQ, 4GRR, 4GRU, 3WNR, 3WNS, 3WNT, 4K9G, 4OSF, 4OYQ, 4P01, 4P0H, 4WR8, 4WRB, 4PKZ, 4PLU, 4TRF, 4TRU, 4XX7, 4XX8, 5BS9, 5BSC, 5BSI, 5EIZ, 5HVV, 5CG4, 5J7Q, 5BSJ, 5HVT, 4PKK, 5B4O, 5HVS, 5J7P

Identifikatori
AliasiMIF
Vanjski ID-jeviOMIM: 153620 MGI: 96982 HomoloGene: 55655 GeneCards: MIF
EC broj5.3.3.12
Lokacija gena (čovjek)
Hromosom 22 (čovjek)
Hrom.Hromosom 22 (čovjek)[1]
Hromosom 22 (čovjek)
Genomska lokacija za Inhibicijski faktor migracije makrofaga
Genomska lokacija za Inhibicijski faktor migracije makrofaga
Bend22q11.23Početak23,894,383 bp[1]
Kraj23,895,227 bp[1]
Lokacija gena (miš)
Hromosom 10 (miš)
Hrom.Hromosom 10 (miš)[2]
Hromosom 10 (miš)
Genomska lokacija za Inhibicijski faktor migracije makrofaga
Genomska lokacija za Inhibicijski faktor migracije makrofaga
Bend10 38.59 cM|10 C1Početak75,695,187 bp[2]
Kraj75,696,074 bp[2]
Ontologija gena
Molekularna funkcija cytokine activity
isomerase activity
GO:0001948, GO:0016582 vezivanje za proteine
chemoattractant activity
phenylpyruvate tautomerase activity
signaling receptor binding
dopachrome isomerase activity
protease binding
GO:0005145 cytokine receptor binding
vezivanje identičnih proteina
Ćelijska komponenta Vezikula
myelin sheath
nukleoplazma
extracellular region
cell surface
Egzosom
citoplazma
citosol
secretory granule lumen
ficolin-1-rich granule lumen
Vanćelijsko
Biološki proces positive regulation of protein phosphorylation
negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediator
positive regulation of MAP kinase activity
carboxylic acid metabolic process
positive regulation of chemokine (C-X-C motif) ligand 2 production
immune system process
positive regulation of fibroblast proliferation
DNA damage response, signal transduction by p53 class mediator
negative regulation of apoptotic process
negative regulation of mature B cell apoptotic process
negative regulation of gene expression
positive regulation of peptidyl-serine phosphorylation
protein homotrimerization
positive regulation of lipopolysaccharide-mediated signaling pathway
cell surface receptor signaling pathway
negative regulation of DNA damage response, signal transduction by p53 class mediator
regulation of cell population proliferation
positive regulation of arachidonic acid secretion
positive regulation of B cell proliferation
positive regulation of peptidyl-tyrosine phosphorylation
positive regulation of prostaglandin secretion involved in immune response
prostaglandin biosynthetic process
Urođeni imunski sistem
negative regulation of myeloid cell apoptotic process
inflammatory response
Ćelijska proliferacija
positive regulation of phosphorylation
positive regulation of myeloid leukocyte cytokine production involved in immune response
leukocyte migration
regulation of macrophage activation
positive regulation of protein kinase A signaling
positive chemotaxis
neutrophil degranulation
interleukin-12-mediated signaling pathway
negative regulation of macrophage chemotaxis
positive regulation of tumor necrosis factor production
positive regulation of ERK1 and ERK2 cascade
regulation of signaling receptor activity
Izvori:Amigo / QuickGO
Ortolozi
VrsteČovjekMiš
Entrez
Ensembl
UniProt
RefSeq (mRNK)

NM_002415

NM_010798

RefSeq (bjelančevina)

NP_002406
NP_002406.1

NP_034928

Lokacija (UCSC)Chr 22: 23.89 – 23.9 MbChr 10: 75.7 – 75.7 Mb
PubMed pretraga[3][4]
Wikipodaci
Pogledaj/uredi – čovjekPogledaj/uredi – miš
Inhibitorni faktor migracije makrofaga (MIF)
Makrofag
Identifikatori
SimbolMIF

Bakterijski antigeni stimuliraju bijela krvna zrnca da otpuste MIF u krvotok.[10] Cirkulirajući MIF se vezuje za CD74 na drugim imunskim ćelijama, kako bi pokrenuo akutni imunski odgovor. Stoga je MIF klasifikovan kao upalni citokin. Štaviše, glukokortikoidi također stimulišu bijela krvna zrnca da oslobađaju MIF i stoga on delimično suprotstavlja inhibitorne efekte koje glukokortikoidi imaju na imunski sistem. Konačno trauma aktivira prednji režanj hipofize da oslobodi MIF.[11]

Aminokiselinska sekvenca

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Dužina polipeptidnog lanca je 115 aminokiseline, a molekulska težina 12 476 Da.[11]

1020304050
MPMFIVNTNVPRASVPDGFLSELTQQLAQATGKPPQYIAVHVVPDQLMAF
GGSSEPCALCSLHSIGKIGGAQNRSYSKLLCGLLAERLRISPDRVYINYY
DMNAANVGWNNSTFA

Struktura

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Inhibicijski faktor migracije makrofaga sastavlja se u trimer od tri identične podjedinice. Svaki od ovih monomera sadrži dva antiparalelna alfa heliksa i četvorolančani beta-list. Monomere okružuju centralni kanal sa trostrukom rotacijskom simetrijom.[12][13]

Odgovor na povredu

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Citokini imaju važnu ulogu u podsticanju zacjeljivanja rana i obnavljanja tkiva. Povreda ćelije dovodi do oslobađanja MIF-a koji zatim stupa u interakciju sa CD74. MIF-CD74 signalizacija aktivira proopstanak i proliferativne puteve koji štite domaćina tokom ozljede.[14]

Enzimska aktivnost

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MIF sadrži dva motiva sa katalitskom aktivnošću. Prvi je motiv od 27 aminokiselina koji se nalazi na N-terminalu funkcioniše kao fenilpiruvat-tautomeraza koja može katalizirati konverziju 2-karboksi-2,3-dihidroindol-5,6-kinona (dopahrom) u 5,6-dihidroksiindol-2-karboksilnu kiselinu (DHICA).[15][16] MIF također sadrži Cys-Ala-Leu-Cys katalitsko mjesto između ostataka 57 i 60 koje funkcionira kao disulfid- reduktaza.[17]

Funkcija

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Ovaj gen kodira limfokin uključen u ćelijski posredovanu imunost, imunoregulaciju i upale.[18][19][20] MIF ima ulogu u regulaciji funkcije makrofaga u odbrani domaćina kroz supresiju protivupalnih efekata glukokortikoida.[20][21][22] Ovaj limfokin i JAB1 protein formiraju kompleks u citosolu blizu periferne plazmamembrane, što može ukazivati na ulogu u integrinskim signalnim putevima.[23]

Mehanizam djelovanja

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MIF se vezuje za CD74,[24] izazivajući njegove fosforilacije i regrutacije CD44 koji zatim aktivira nereceptorske tirozin kinaze, što u konačnici dovodi do fosforilacije kinaza reguliranih vanćelijskim signalom.[25] Osim ERK-a, stimulacija CD74 aktivira i druge signalne puteve kao što su PI3K-Akt, NF-κB i AMP-aktivirani putevi protein kinaze (AMPK).[26]

Interakcije

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Zabilježeno je da inhibitorni faktor migracije makrofaga ima interakcije sa:

Klinički značaj

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MIF je potencijalni cilj lijeka za sepsu, reumatoidni artritis i rak.[40][41]

Parazitno-proitvedeni homolozi MIF-a

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MIF citokin proizveden parazitima u imunskoj evaziji, invaziji i patogenezi

Višestruki protozojski paraziti proizvode homologe MIF-a koji imaju slične upalne funkcije kao i ljudski MIF i imaju ulogu u njihovoj patogenezi, invaziji i imunskoj evaziji.[42][43] Pretklinička studija je pokazala da blokiranje parazitskog MIF poboljšava ishod kod teških infekcija protozoaama.[44] Prijavljeni primjeri protozoa sa homolozima MIF-a:

Reference

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Vanjski linkovi

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